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A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
scientific article published on 14 June 2006
Author/s
author: Michael Barmada, Tanya M Teslovich, Jeffrey Trent
Work details
Publication date
June 14, 2006
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Language
English
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